Torthaí cuardaigh - Fabrizio Tagliavini
- 1 - 20 toradh as 102 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutations de réir Giacomina Rossi, Fabrizio Tagliavini
Foilsithe / Cruthaithe 2015Revisão -
2
Detection of Misfolded Aβ Oligomers for Sensitive Biochemical Diagnosis of Alzheimer’s Disease de réir Natalia Salvadores, Mohammad Shahnawaz, Elio Scarpini, Fabrizio Tagliavini, Claudio Soto
Foilsithe / Cruthaithe 2014Artigo -
3
PRP27–30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets de réir Francesco Perini, Rubén Vidal, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli
Foilsithe / Cruthaithe 1996Artigo -
4
Codeposition of Cystatin C with Amyloid-β Protein in the Brain of Alzheimer Disease Patients de réir Efrat Levy, Magdalena Sastre, Asok Kumar, Gloria Gallo, Pedro Piccardo, Bernardino Ghetti, Fabrizio Tagliavini
Foilsithe / Cruthaithe 2001Artigo -
5
Substitutions at Codon 22 of Alzheimer's Aβ Peptide Induce Diverse Conformational Changes and Apoptotic Effects in Human Cerebral Endothelial Cells de réir Leticia Miravalle, Takahiko Tokuda, Roberto Chiarle, Giorgio Giaccone, Orso Bugiani, Fabrizio Tagliavini, Blas Frangione, Jorge Ghiso
Foilsithe / Cruthaithe 2000Artigo -
6
Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein. de réir Luca De Gioia, Carlo Selvaggini, Elena Ghibaudi, Luisa Diomede, Orso Bugiani, Gianluigi Forloni, Fabrizio Tagliavini, Mario Salmona
Foilsithe / Cruthaithe 1994Artigo -
7
Endogenous Proteolytic Cleavage of Normal and Disease-Associated Isoforms of the Human Prion Protein in Neural and Non-Neural Tissues de réir Adolfo Jiménez‐Huete, Patricia Lievens, Rubén Vidal, Pedro Piccardo, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli
Foilsithe / Cruthaithe 1998Artigo -
8
Identification of a second bovine amyloidotic spongiform encephalopathy: Molecular similarities with sporadic Creutzfeldt-Jakob disease de réir Cristina Casalone, Gianluigi Zanusso, Pier Luigi Acutis, Sérgio Ferrari, Lorenzo Capucci, Fabrizio Tagliavini, Salvatore Monaco, Maria Caramelli
Foilsithe / Cruthaithe 2004Artigo -
9
O3‐06‐06: ANTI‐Aβ AUTOANTIBODIES IN CAA AND AD: DIFFERENT SINGERS FOR THE SAME ARIA? de réir Fabrizio Piazza, Steven M. Greenberg, Alberto Lleó, Carlo Ferrarese, Ricardo Nitríni, Fabrizio Tagliavini, Jacopo C. DiFrancesco
Foilsithe / Cruthaithe 2014Artigo -
10
Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease de réir Luis Concha‐Marambio, Sandra Pritzkow, Fabio Moda, Fabrizio Tagliavini, James W. Ironside, Paul E. Schulz, Claudio Soto
Foilsithe / Cruthaithe 2016Artigo -
11
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58. de réir Fabrizio Tagliavini, Frances Prelli, Jorge Ghiso, Orso Bugiani, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Blas Frangione
Foilsithe / Cruthaithe 1991Artigo -
12
Diagnostic differentiation of mild cognitive impairment due to Alzheimer's disease using a hippocampus-dependent test of spatial memory de réir Kuven Moodley, Ludovico Minati, Valeria Elisa Contarino, Sara Prioni, Ruth Wood, Rebecca Cooper, Ludovico D’Incerti, Fabrizio Tagliavini, Dennis Chan
Foilsithe / Cruthaithe 2015Artigo -
13
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred. de réir Giorgio Giaccone, Laura Verga, Orso Bugiani, B Frangione, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Fabrizio Tagliavini
Foilsithe / Cruthaithe 1992Artigo -
14
Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation de réir Laura Canafoglia, Michela Morbin, V. Scaioli, Davide Pareyson, Ludovico D’Incerti, Valeria Fugnanesi, Fabrizio Tagliavini, Samuel F. Berkovic, Silvana Franceschetti
Foilsithe / Cruthaithe 2014Artigo -
15
The Efficacy of Tetracyclines in Peripheral and Intracerebral Prion Infection de réir Ada De Luigi, Laura Colombo, Luisa Diomede, Raffaella Capobianco, Michela Mangieri, Claudia Miccolo, Lucia Limido, Gianluigi Forloni, Fabrizio Tagliavini, Mario Salmona
Foilsithe / Cruthaithe 2008Artigo -
16
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro. de réir Fabrizio Tagliavini, Frances Prelli, Laura Verga, Giorgio Giaccone, R. Sarma, P D Gorevic, Bernardino Ghetti, F Passerini, Elena Ghibaudi, Gianluigi Forloni
Foilsithe / Cruthaithe 1993Artigo -
17
A new function of microtubule-associated protein tau: Involvement in chromosome stability de réir Giacomina Rossi, Leda Dalprà, Francesca Crosti, Sara Lissoni, Francesca L. Sciacca, Marcella Catania, Michela Mangieri, Giorgio Giaccone, Danilo Croci, Fabrizio Tagliavini
Foilsithe / Cruthaithe 2008Artigo -
18
Prion Protein Amyloidosis de réir Bernardino Ghetti, Pedro Piccardo, B Frangione, Orso Bugiani, Giorgio Giaccone, Katherine Young, Frances Prelli, Martin R. Farlow, Stephen R. Dlouhy, Fabrizio Tagliavini
Foilsithe / Cruthaithe 1996Revisão -
19
Defined α-synuclein prion-like molecular assemblies spreading in cell culture de réir Suzana Aulić, Tran Thanh Nhat Le, Fabio Moda, Saïda Abounit, Stefania Corvaglia, Loredana Casalis, Stefano Gustincich, Chiara Zurzolo, Fabrizio Tagliavini, Giuseppe Legname
Foilsithe / Cruthaithe 2014Artigo -
20
The Semantic Variant of Primary Progressive Aphasia: Clinical and Neuroimaging Evidence in Single Subjects de réir Leonardo Iaccarino, Chiara Crespi, Pasquale Anthony Della Rosa, Eleonora Catricalà, Lucia Guidi, Alessandra Marcone, Fabrizio Tagliavini, Giuseppe Magnani, Stefano F. Cappa, Daniela Perani
Foilsithe / Cruthaithe 2015Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Disease
Pathology
Biology
Dementia
Gene
Genetics
Frontotemporal dementia
Internal medicine
Neuroscience
Biochemistry
Prion protein
Psychology
C9orf72
Alzheimer's disease
Amyloid (mycology)
Chemistry
Virology
Mutation
Scrapie
Phenotype
Atrophy
Frontotemporal lobar degeneration
Magnetic resonance imaging
Radiology
Cell biology
Cognition
Genotype
Immunology
Molecular biology